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rs876660228

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876660228(-;-)
Make rs876660228(-;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32339552
GeneBRCA2
is asnp
is mentioned by
dbSNPrs876660228
ebirs876660228
HLIrs876660228
Exacrs876660228
Varsomers876660228
Maprs876660228
PheGenIrs876660228
hapmaprs876660228
1000 genomesrs876660228
hgdprs876660228
ensemblrs876660228
gopubmedrs876660228
geneviewrs876660228
scholarrs876660228
googlers876660228
pharmgkbrs876660228
gwascentralrs876660228
openSNPrs876660228
23andMers876660228
23andMe allrs876660228
SNP Nexus

SNPshotrs876660228
SNPdbers876660228
MSV3drs876660228
GWAS Ctlgrs876660228
Max Magnitude0
ClinVar
Risk rs876660228(;)
Alt rs876660228(;)
Reference rs876660228(TC;TC)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32913689_32913690delTC
CLNSRC
CLNACC RCV000218209.1,